BRCA1, Histone H2AX Phosphorylation, and Male Meiotic Sex Chromosome Inactivation

Male 0301 basic medicine Sex Chromosomes Agricultural and Biological Sciences(all) Biochemistry, Genetics and Molecular Biology(all) Reverse Transcriptase Polymerase Chain Reaction Blotting, Western Genes, BRCA1 Cell Cycle Proteins Ataxia Telangiectasia Mutated Proteins Protein Serine-Threonine Kinases Chromatin Assembly and Disassembly Immunohistochemistry Histones Mice 03 medical and health sciences Mutation Animals Immunoprecipitation Pachytene Stage Phosphorylation In Situ Hybridization, Fluorescence DNA Primers Oligonucleotide Array Sequence Analysis
DOI: 10.1016/j.cub.2004.11.032 Publication Date: 2004-12-14T13:56:07Z
ABSTRACT
In mammalian spermatogenesis, the X and Y chromosomes are transcriptionally silenced during the pachytene stage of meiotic prophase (meiotic sex chromosome inactivation, MSCI), forming a condensed chromatin domain termed the sex or XY body. The nucleosomal core histone H2AX is phosphorylated within the XY chromatin domain just prior to MSCI, and it has been hypothesized that this triggers the chromatin condensation and transcriptional repression. Here, we show that the kinase ATR localizes to XY chromatin at the onset of MSCI and that this localization is disrupted in mice with a mutant form of the tumor suppressor protein BRCA1. In the mutant pachytene cells, ATR is usually present at nonsex chromosomal sites, where it colocalizes with aberrant sites of H2AX phosphorylation; in these cells, there is MSCI failure. In rare pachytene cells, ATR does locate to XY chromatin, H2AX is then phosphorylated, a sex body forms, and MSCI ensues. These observations highlight an important role for BRCA1 in recruiting the kinase ATR to XY chromatin at the onset of MSCI and provide compelling evidence that it is ATR that phosphorylates H2AX and triggers MSCI.
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